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1.

Acrocapitofemoral dysplasia

Acrocapitofemoral dysplasia (ACFD) is an autosomal recessive skeletal dysplasia characterized by postnatal-onset disproportionate short stature, relatively large head, narrow thorax, lumbar lordosis, short limbs, and brachydactyly with small broad nails (Ozyavuz Cubuk and Duz, 2021). [from OMIM]

MedGen UID:
334681
Concept ID:
C1843096
Disease or Syndrome
2.

Spondyloepimetaphyseal dysplasia, Shohat type

Shohat-type spondyloepimetaphyseal dysplasia (SEMDSH) is a chondrodysplasia characterized by vertebral, epiphyseal, and metaphyseal abnormalities, including scoliosis with vertebral compression fractures, flattened vertebral bodies, and hypomineralization of long bones. Affected individuals may exhibit a small trunk, short neck, small limbs, joint laxity, bowlegs, and/or abdominal distention with hepatosplenomegaly (summary by Egunsola et al., 2017). [from OMIM]

MedGen UID:
400703
Concept ID:
C1865185
Disease or Syndrome
3.

Fibular overgrowth

Relatively increased growth of the fibula compared to that of the tibia. [from HPO]

MedGen UID:
350389
Concept ID:
C1864298
Finding
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